Nuclear spin-spin coupling via nonbonded interactions. III. Effects of

Aug 1, 1975 - III. Effects of molecular structure on through-space fluorine-fluorine and hydrogen-fluorine coupling ... Mark D. Struble , Maxwell Garg...
0 downloads 0 Views 297KB Size
4770 (2) L. K. Montgomery and L. E. Applegate. J. Am. Chem. SOC.. 89, 2952 (1967); L. K. Montgomery, A. 0. Clorese, A. M. Crelier, and L. E. Applegate, ibid., 89, 3453 (1967); L. K. Montgomery, F. Scardiglia, and J. D. Roberts. /bid, 87, 1917 (1965); L. K. Montgomery and J. D. Roberts, ibid., 82, 4750 (1960); F. Scardiglia and J. D. Roberts, Tetrahedron, 1. 343 (1957); 0. Wittig and G. Harborth. Chem. Ber., 77, 306 (1944); see also G. Wiltig. J. Weinlich. and E. R. Wilson, Chem. Ber.. 98, 458 (1965); G. Wittig and P. Fritz, Angew. Chem., Int. Ed. Engl., 5, 846 (1966); A. T. Bottini, F. P. Corson, R. Fitzgerald. and K. A. Frost, Ill, Tetrahedron, 28, 4883 (1972); G. Wittig and J. Heyn, Justus Liebigs Ann. Chem., 758, 1 (1972); G. Kobrich, Angew. Chem., Int. Ed. Engl., 11, 473 (1972). (3) For a general review see R . W. Hoffmann, "Dehydrobenzene and Cycloalkanes". Academic Press, New York, N.Y., 1967, Chapter 8. (4) P. G. Gassman, J. P. Andrews, Jr.. and D. S . Patton, J. Chem. SOC.. Chem. Commun.. 437 (1969). (5) P. G. Gassman and T. J. Atkins, J. Am. Chem. SOC..92, 5810 (1970). In addition to 3, 7 % of 2-phenylnortricyclane was formed. A carbenoid intermediate was proposed. (6) P. G. Gassman and T. J. Atkins. Tetrahedron Lett., in press. (7) The tetrahydrofuran solutions of n-butyllithium were prepared immediately prior to use by stripping the solvent from a hexane solution of nbutyllithium under vacuum and then replacing the hexane with tetrahydrofuran. Fortunately, our reactions were clean and rapid in tetrahydrofuran and were complete prior to destruction of the n-butyllithium through reaction with the solvent. For a discussion of such reactions see H. Gilman and B. S. Goj, J. Org. Chem.. 23, 1165 (1957). (8) Control experiments have shown that treatment of 2-n-butylbicyclo[2.2. 1]heptene under the reaction conditions, followed by quenching with deuterium oxide, dd not result in deuterium incorporation. (9) The details of the preparation of labeled 1 will be presented in a full paper on this subject. (10) R. N. McDonald and R . N. Steppel, J. Am. Chem. Soc.. 92, 5664 (1970). (11) The absolute configuration of 4 was assigned on the basis of the absolute configuration of (-)-(2F+3-methyltricyclo[ 2.2.1 .02,B]heptaneas assigned by J. A. Berson and R. G. Bergman. J. Am. Chem. SOC., 89, 2569 (1967). The assumption was made that both the n-butyl and methyl substituted derivatives would have the same sign of rotation for the same absolute configuration since this alkyl substitution contributed the only chiral factor to an otherwise symmetrical skeleton. (12) The mechanism whereby the other 15% is derived remains to be elucidated. Presumably this occurs through some type of direct coupling reaction since retention of stereochemistry is observed. (13) Unsuccessful attempts to prepare cyclobutyne have been reported: L. K. Montgomery and J. D.Roberts, J. Am. Chem. SOC.,82,4750 (1960); G. Wittig and E. R. Wilson, Chem. Ber., 98, 451 (1965). (14) Address correspondence concerning this report to P.G.G. at the Univarsity of Minnesota.

Paul G . Gas~rnan*'~ Joseph J. Valcho Department of Chemistry, The Ohio State University Columbus, Ohio 43210 Department of Chemistry, University of Minnesota Minneapolis, Minnesota 55455 Received March 31. 197.5

Nuclear Spin-Spin Coupling via Nonbonded Interactions. 111. Effects of Molecular Structure on Through-Space Fluorine-Fluorine and H ydrogen-Fluorine Coupling' Sir:

The concept2 that certain intramolecularly crowded atoms can experience nuclear spin-spin coupling predominantly via through-space (or direct) nonbonded interactions of the two atoms, as opposed to interactions involving the intervening bonds, continues to receive considerable attention. Many examples have been reported for both FF3x4and H F2a,5 coupling, and several theoretical treatments have Some initial findings of the systematic investigations we a r e undertaking of through-space coupling in polynuclear aromatic systems are presented in C h a r t Thc values of J F Fobserved for 1-69 support the idea that the magnitude of through-space FF coupling depends on the internuclear distance. For example, the FF distance in the difluorophenanthrene 2 obviously is shorter than that in the difluoronaphthalene 1, which accounts for J F Fbeing much larger for 2 than for 1. In the series of difluoro compounds 2-5, the sharply decreasing values of J F F (2, 174 Hz;" 3, Journal of the American Chemical Society

/

97.1 6

qw

Chart I. Through-space FF and HF coupling constants for compounds 1-9. ~

00

(yy 00

00

0 0; CH 00

A

0 0:' 00

0 0 00 H'l

43.2 Hz;" 4, 5.3 Hz;I2 5, ca. 0 Hz) are consistent with the expectation that out-of-plane distortions in these helical molecules give rise to increasing FF distances in the sequence 2 < 3 < 4 < 5. The observation of the same J F F value of 174 H z for both the benzo[ghi]perylene derivative 612 and the phenanthrene derivative 2 reflects the similar spatial relationship of the two fluorines in these compounds. Coupling between bay hydrogen and fluorine nuclei in 4fluorophenanthrenes has apparently not been reported previously. In addition to the value of 2.6 Hz13 for the coupling between H-5 and F-4 in 4-fluorophenanthrene (7) itself, we find the following values of 5 5 4 for seven different substituted derivatives of 7:14 %methyl, 2.9 Hz; 8-chloro, 3.8 Hz; 6fluoro, 3.8 Hz; 6-chloro, 4.4 Hz; 6-bromo, 4.4 Hz; 6-methoxy, 4.6 Hz; and 7-fluoro-l-methyl, 4.6 H z . To our knowledge, the value of 14.5 H z L 2for the coupling between H - I 2 and F-l in 1-fluorobenzo[c]phenanthrene (8) exceeds in magnitude all previously reported values for throughspace H F coupling via nonbonded i n t e r a ~ t i 0 n s . IW ~ e also find the following values of J12.1 for four different substituted derivatives of 8:7 9-methoxy, 14.6 Hz; 9-bromo, 14.7 Hz; 9-cyano, 15.3 Hz; and IO-fluoro-8-methyl, 14.3 Hz. A value of 1.7 H z is found for the coupling constant for H-1 1 and F-IO in IO-fluorodibenzo[c,g]phenanthrene(9) and also in its 13-flUOrO-I -methyl derivative. The patterns of our F F and H F coupling results show one striking and instructive feature as illustrated graphically in Figure 1: the magnitudes of the H F coupling constants in 7-9 run qualitatively parallel to those of the F F coupling constants i n 1-3, respectively, and there is no such parallelism for what might have been regarded as the structurally more comparable systems 7-9 and 2-4, respectively. For example, the largest value of J F F in the series 1-4 is found in the phenanthrene systtxn 2, whereas the largest value of J H F in the series 7-9 is found not in the, corresponding phenanthrene system 7 but rather in the benzo[c]phenanthrene system 8. W e believe this provides evidence for the concept that the nonbonded interactions of importance for through-space H F coupling a r e not those between F and H

/ August 6 , I975

477 1

1

1

I 200

1

2

4

2o

I

I

I

5

6

7

n

Figure 1. Values of J F F(circles, left-hand ordinate) for compounds 1-4 and J H F(squares, right-hand ordinate) for H-5, H-12, and H - l l i n compounds 7-9, respectively, plotted against n, where n i s the number of bonds along the shortest pathway through the molecular framework that connects the two fluorines i n 1-4 or that connects the fluorine and the carbon bearing the coupled hydrogen i n 7-9. The number o f connecting bonds n i s used here merely as an index of structural type in these polynuclear systems; coupling through these bonds is considered negligible i n magnitude for all cases except 1 and 7, i n which small through-bond contributions to the observed coupling cannot be ruled out.

directly, since those interactions presumably would be optimized in 7 just as the F F interactions are evidently optimized in 2, but rather are those between F and the carbon to which the H is attached.I6 Thus, we conclude that the large value of JHFfor the benzo[c]phenanthrene 8 results from an especially favorable spatial relationship between F-1 and C-12 in 8, analogous to the especially favorable spatial relationship between F-4 and F-5 that gives rise to in the phenanthrene 2. the large value of JFF

Acknowledgment is made to the donors of The Petroleum Research Fund, administered by the American Chemical Society, and to the National Science Foundation (GP10640) for support of this research.

L. M. Stock and M. R . Wasielewski, J. Org. Chem., 35, 4240 (1970); (u) K. L. Servis and F. R. Jerome, J. Am. Chem. Soc.. 03, 1535 (1971); (v) S.Ng, J. Chem. Soc.A, 1586 (1971);(w) H. M. Hutton, J. B. Rowbotham, B. H. Barber. and T. Schaefer, Can. J. Chem., 40, 2033 (1971); (x) W. Adcock. D. G. Matthews, and S. Q. A. Rizvi, Aust. J. Chem., 24, 1829 (1971); (y) E. Abushanab, J. Am. Chem. Soc., 03, 6532(1971);(z) A. B. Foster, R. Hems, and J. H. Westwood, Carbohyd. Res.. 23, 316 (1972);(aa) W. B. Smith, D. L. Deavenport, and A. M. Ihrig. J. Am. (bb) I. Agranat, M. Rabinovitz, I. Gosnay. Chem. Soc., 04, 1959 (1972); (cc) F. R. Jerome and K. and A. Weitzen-Dagan, ibid., 04, 2889 (1972); L. Servis, ibid., 04. 5896 (1972);(dd) P. Martinson. Acta Chem. Scand., 28, 3529 (1972); (ee) P. A. Lehmann F. and L. F. Johnson, Org. Magn. Reson., 5, 61 (1973);(ff) H. C. Clark and L. E. Manzer, J. Chem. Soc., Chem. Commun., 870 (1973);(gg) W. Adcock and S.Q. A. Rizvi, Aust. J. Chem., 28, 2659 (1973);(hh) G. HAgele and M. Weidenbruch, Org. Maan. Reson.. 8. 66 11974);(ii) H. Fritz and T. Winkler, Helv. Chim. A&, 57, 836 (1974). (a) M. Barfield and M. Karplus, J. Am. Chem. Soc.. 01, 1 (1969);(b) K. Hirao, H. Nakatsuji, H. Kato, and T. Yonezawa, ibid., 94, 4078 (1972); (c) K. Hirao, H. Nakatsujl, and H. Kato, ibid., 05, 31 (1973);(d) for MUtionarv remarks reaardina ref 6b and c see J. Hitton and L. H. Sutcliffe. J. Magn. Reson.. 15, 241-(1974);(e) A. D. Buckingham and J. E. Cordle. J. Chem. Soc., Faraday Trans. 2, 994 (1974);(f) M. Barfield. A. M. Dean, C. J. Fallick, R. J. Spear, S. Sternhell. and P. W. Westerman, J. Am. Chem. Soc.,07, 1482 (1975). Except as noted, values of &F and Jw were determined from 18F spectra at 56.4MHz and ’H spectra at 60 MHz in CeD6 solution. Full synthetic details for all new compounds will be reported later. Nomenclature: 1, 4,5difluoro-l-methylnaphthene; 2, 4,5difluoro-lmethylphenanthrene: 3, 1,12difluoro-4-methylbenzo[ clphenanthrene: 4, 10,lldifluoro-1-methyMibenzo[c,g]phenanthrene;5, 9,12difluoro1-methyMibenzo[c,g]phenanthrene; 8,7,8difluorc- 1-methylbenzo[ghilperylene. Values of 167-170 Hz have been reported previously for JFF in several 1,8disubstituted-4.5difluorophenanthrenes by K. L. Servis and K.-N. Fang, J. Am. Chem. Soc., 00,6712 (1968). The 5-methyl isomer of 3 has a &F value of 45.3Hz. The I8F spectra of 4 and 8 were measured in DMF at 94.1MHz; the ‘H spectrum of 8 was measured in C6D6 at 100 MHz. We are grateful to Professor David R. Dalton of Temple University for obtaining these spectra. The signal for H-5 in the ’H spectrum of 7 was simplified to a 2.6-Hz doublet (also 2.6 Hz in CC14) by decoupling all the other hydrogens. Measured in CC4 solution. Values of &F up to 16 Hz have been reported for the NH hydrogens in some 2-fluorobenzamide derivatives in which the nuclear spin information is thought to be transmitted through intramolecular HF hydrogen

bond^.^"

This concept has been suggested previously on the basis of HF coupling studies involving aliphatic hydrogen^.^"^^^^^ See also ref 5ee. (a) This work is taken in part from the Ph.D. Thesis of W.M.R.. Bryn Mawr College, 1974;(b) National Science Foundation Trainee, 19691970,and U.S. Steel Foundation Fellow, 1970-1972.

-

Frank B. Mallory,* Clelia W. Mallory, Wendella M. Ricker” Department of Chemistry, Bryn Mawr College Bryn Mawr, Pennsyluania 19010 Received April 21, 1975

References and Notes (1) (a) Part I, F. B. Mallory, J. Am. Chem. SOC., 05, 7747 (1973);(b) part 11, F. B. Mallory. C. W. Mallory, and M.-C. Fedarko, ibid., OS, 3536 (1974). (2)(a) D. R . Davis, R. P. Lutz, and J. D. Roberts. J. Am. Chem. SOC., 83, 246 (1961);(b) L. Petrakis and C. H. Sederholm. J. Chem. fhys., 35, 1243 (1961);(c) S.Ng and C. H. Sederholm. ibid., 40, 2090 (1964). (3)See parts Ila and Illb and references cited therein. (4)For further examples, see (a) E. G. Finer and R. K. Harris, Spectrochim. Acta, Part A, 24, 1939 (1968); (b) L. H. Sutcliffe and B. Taylor, ibid., 28, 619 (1972);(c) R. E. Banks, K. Mullen, W. J. Nicholson, C. Oppenheim, (d) R. D. and A. Prakash. J. Chem. Soc., Perkin Trans. 1, 1098 (1972); Chambers, R. P. Corbally. W. K. R. Musgrave, J. A. Jackson, and R. S. Matthews, ibid., 1286 (1972);(e) M. G. Barlow, R. N. Haszeldine. W. D. Morton, and D. R. Woodward, ibid., 2170 (1972); (f) W. A. Sheppard and D. W. Ovenall, Org. Magn. Reson., 4, 695 (1972);(g) R. D. Chambers and M. Y. Gribble, J. Chem. Soc., Perkin Trans. 1, 1405 (1973);(h) S.L. Bell, R. D. Chambers, M. Y. Gribble, and J. R. Maslakiewicz, ibid., 1716 (1973);(i)R. D. Chambers, R. P. Corbally. T. F. Holmes, and W. K. R. Musgrave, ibid., 108 (1974);(j) R. D. Chambers, M. Clark, J. R. Maslakiewicz, W. K. R. Musgrave, and P. G. Urben, ibid., 1513 (1974). (5) (a) M. T. Rogers and J. C. Woodbrey, J. Phys. Chem., 88, 540 (1962); (b) A. D. Cross and P. W. Landis. J. Am. Chem. Soc.. 84, 1736 (1962); (c) M. Takahashi. D. R. Davis, and J. D. Roberts, ibid., 84, 2935 (1962); (d) A. D. Cross and P. W. Landis, ibid., 84, 3784 (1962);(e) A. G.Massey, E. W. Randall, and D. Shaw. Chem. Ind. London, 1244 (1963); (f) M. S.Newman. R. G. Mentzer, and G. Slomp, J. Am. Chem. SOC., 85, 4018 (1963);(g) A. H. Lewin, ibid., 88, 2303 (1964);(h)A. D. Cross and P. W. (j) Landis, ibid., 88, 4005 (1964);(i)A. D. Cross, ibid., 88, 4011 (1964); J. Burdon, Tetrahedron, 21, 1101 (1965);(k) P. C. Myhre, J. W. Edmonds, and J. D. Kruger, J. Am. Chem. Soc., 88, 2459 (1966); (I)Yu. A. Cheburkov. Yu. A. Aronov, E. I. Fedin, P. V. Petrovskii. and I. L. Knun(m) J. P. N. Brewer. H. yants, Dokl. Akad. Nauk SSSR, 189, 128 (1966); Heaney, and B. A. Marples. Chem. Commun.. 27 (1967);(n) C. W. Jefford, D. T. Hill, L. Ghosez. S. Toppet. and K. C. Ramey. J. Am. Chem. Soc.. 01, 1532 (1969);( 0 ) R Filler and E. W. Choe, ibid., 01, 1862 (1969);(p) A. J. Oliver and W. A. G. Graham, J. Organornet. Chem., 19, 17 (1969);(4)G. W. Gribble and J. R. Douglas, Jr.. J. Am. Chem. Soc.. 02, 5764 (1970);(r) P. A. Lehmann F., Org. Magn. Reson.. 2, 467 (1970);(s) F. Vogtle and P. Neumann, Tetrahedron, 28, 5299 (1970);(t)

Flash Pyrolysis of cy-(p-Tolylsulfonyl)phenyldiazomethane.Carbene Formation by Loss of Sulfur Dioxide’ Sir:

This communication is prompted by our discovery of the apparent expulsion of sulfur dioxide from a sulfene. Such extrusion reactions were postulated over 60 years ago,* but no example has withstood close attention. As remarked in a recent cogent re vie^,^ loss of sulfur dioxide from a sufene is “conspicuously absent”, and all earlier attempts to use external addition reactions to trap the carbene so formed have failed.2s4-6 The Wolff-like rearrangement of sulfonyl carbenes to give sulfenes is known’ and our interest in carbene chemistry and the use of gas-phase reactions of carbenes8 in synthesis led us to examine the flash pyrolysis of cY-(p-tolylsulfony1)phenyldiazomethane ( l).9 It was our thought that a carbene might be trapped more successfully by an internal reaction rather than an external addition, and we further hoped that the two benzene rings would render the fragmentation substantially less endothermic than the 55-60 kcal/mol estimated for the cleavage of Communications to the Editor